Variant (rsID / SNP)

rs17038942

rs17038942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM43. Location: chromosome 3, position 14,172,827. Clinical significance in the table: Benign.

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Reference-table entries

TMEM43Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:14172827
Cytoband: 3p25.1
HGVS: NM_024334.3(TMEM43):c.298-253C>T
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.